108082-57-1 Usage
Description
(1S)-2,2-dimethyl-1-phenylpropan-1-aminium chloride, commonly known as ephedrine, is a medication and stimulant with a range of potential medical applications. It is a sympathomimetic amine that functions as a central nervous system stimulant, increasing heart rate and blood pressure while also dilating bronchial passages.
Uses
Used in Pharmaceutical Industry:
(1S)-2,2-dimethyl-1-phenylpropan-1-aminium chloride is used as a medication for treating low blood pressure, asthma, and congestion due to its ability to stimulate the central nervous system and dilate bronchial passages.
Used in Weight Loss Applications:
Ephedrine is used as a weight loss aid, as it can increase heart rate and blood pressure, potentially leading to increased metabolism and calorie burning.
Used in Performance Enhancement:
(1S)-2,2-dimethyl-1-phenylpropan-1-aminium chloride is used as a performance enhancer, as its stimulant properties can improve physical performance and reduce fatigue.
However, it is important to note that ephedrine can have significant side effects and interactions with other medications, and its use is regulated in many countries due to its potential for abuse and dependence.
Check Digit Verification of cas no
The CAS Registry Mumber 108082-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,8 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108082-57:
(8*1)+(7*0)+(6*8)+(5*0)+(4*8)+(3*2)+(2*5)+(1*7)=111
111 % 10 = 1
So 108082-57-1 is a valid CAS Registry Number.
108082-57-1Relevant articles and documents
Enantioselective hydrogenation of N-H imines
Hou, Guohua,Gosselin, Francis,Li, Wei,McWilliams, J. Christopher,Sun, Yongkui,Weisel, Mark,O'Shea, Paul D.,Chen, Cheng-Yi,Davies, Ian W.,Zhang, Xumu
supporting information; experimental part, p. 9882 - 9883 (2009/12/06)
(Figure Presented) N-H ketoimines 3a-3v are readily prepared in high yield via organometallic addition to nitriles and isolated as corresponding bench-stable hydrochloride salts. Homogeneous asymmetric hydrogenation of unprotected N-H ketoimines 3a-3v usi
